Package 0404-9921-02

Brand: NALOXONE HYDROCHLORIDE

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9921-02
Digits Only 0404992102
Product NDC 0404-9921
Product ID 0404-9921_08021e60-380c-4a63-a943-00b3dec83ced
Description

1 BOX in 1 BAG (0404-9921-02) / 1 SYRINGE in 1 BOX / 2 mL in 1 SYRINGE

Marketing

Marketing Status
Discontinued 2026-02-28
Brand NALOXONE HYDROCHLORIDE
Generic naloxone hydrochloride
Sample Package No

Linked Drug Pages (1)

NALOXONE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["PARENTERAL"], "spl_id": "08021e60-380c-4a63-a943-00b3dec83ced", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191250"], "spl_set_id": ["6d8e0730-f224-4186-9927-6acce7d3392b"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOX in 1 BAG (0404-9921-02)  / 1 SYRINGE in 1 BOX / 2 mL in 1 SYRINGE", "package_ndc": "0404-9921-02", "marketing_end_date": "20260228", "marketing_start_date": "20220118"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "0404-9921_08021e60-380c-4a63-a943-00b3dec83ced", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0404-9921", "generic_name": "naloxone hydrochloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALOXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA072076", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20220118"}